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http://rdf.disgenet.org/nanopublications.trig#NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_assertion
;
np:hasProvenance
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_provenance
;
np:hasPublicationInfo
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_assertion
a
np:Assertion
.
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_provenance
a
np:Provenance
.
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_assertion
{
miriam-gene:4049
a
ncit:C16612
.
lld:C2733225
a
ncit:C7057
.
dgn-gda:DGN81dd23d741bb946fb422b63a4d29f019
sio:SIO_000628
miriam-gene:4049
,
lld:C2733225
;
a
sio:SIO_001121
.
}
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_provenance
{
dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_assertion
dcterms:description
"[Thus, further to the recent finding that LTA gene variation is associated with susceptibility to coronary heart disease, the present study provides evidence of an association between LTA genotype and the extent of coronary atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15973460
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP219444.RAf8sNQslRW49qJBbFCAeN7HC0NuhInHMMq2HeFJI7Hpg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}